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Vol 17, No 4 (2020)
A clinical case of the X-linked moesin deficiency
Latysheva T.V., Latysheva E.A., Setdikova N.H., Esaulova D.R.
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(Rus)
Vol 9, No 4 (2012)
Clinical and laboratory phenotypes of severe combined immunodeficiencies with mutations in RAG1/RAG2 genes
Kondratenko I.V., Pashchenko O.E., Rodina Y.A., Belevtcev M.V., Van d.M., Bologov A.A.
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(Rus)
Vol 17, No 3 (2020)
Federal clinical guidelines. Primary immunodeficiency: severe combined immunodeficiency
Rodina Y.A., Deripapa E.V., Laberko A.L., Pershin D.E., Kalinina E.V., Raikina E.V., Roppelt A.A., Yukhacheva D.V., Burlakov V.I., Balashov D.N., Rumiantsev A.G., Shcherbina A.Y.
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(Rus)
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